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Chemical Structure| 883233-85-0 Chemical Structure| 883233-85-0

Structure of 883233-85-0

Chemical Structure| 883233-85-0

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Product Details of [ 883233-85-0 ]

CAS No. :883233-85-0
Formula : C3H3BrF2O
M.W : 172.96
SMILES Code : O=C(CBr)C(F)F
English Name :3-Bromo-1,1-difluoropropan-2-one
MDL No. :MFCD16878954

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Application In Synthesis of [ 883233-85-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 883233-85-0 ]

[ 883233-85-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 15884-86-3 ]
  • [ 883233-85-0 ]
  • [ 1294001-18-5 ]
YieldReaction ConditionsOperation in experiment
40% In N,N-dimethyl-formamide at 100℃; 1.1.7 To a solution of 5-(methoxymethyl)-1 ,3,4-thiadiazol-2-amine (CAS: 15884-86-3, 1.0 eq., 6.5 g, 45 mmol) in DMF (100 ml_), at 100°C, was added dropwise a solution of 3-bromo- 1 ,1-difluoro-propan-2-one (CAS: 883233-85-0, 1.05 eq., 8.1 g, 47 mmol) in DMF (5 ml_). The reaction mixture was heated at 100°C during 3 h and the completion was checked by LC/MS. A saturated aqueous solution of NaHCC>3 was added and the organic layer was extracted with ethyl acetate (three times). The combined organic layers were washed with water (five times), dried over MgSCU, filtered and evaporated to dryness to give a brown solid (7.6 g). The crude was purified by flash chromatography Biotage Isolera Four (100 g KP-SNAP silica gel column in a gradient of 0% to 5% methanol in dichloromethane over 12 CV) and the pure fractions were combined and evaporated under high vacuum to give 6-(difluoromethyl)-2-(methoxymethyl)imidazo[2,1- b][1 ,3,4]thiadiazole VII (3.95 g, 17.8 mmol) as an orange solid. Yield: 40% LC/MS: [M+H]+ = 220.2 1H NMR (400 MHz, DMSO-c/6): δ 8.53 (t, J = 2.2 Hz, 1 H), 7.01 (t, J = 54.6 Hz, 1 H), 4.83 (s, 2H), 3.43 (s, 3H).
40% In N,N-dimethyl-formamide at 100℃; for 3h; 2.1.5 1.5 Synthesis of 6-(difluoromethyl)-2-(methoxymethyl)imidazo[2, 1 b][1 ,3,4]thiadiazole VII To a solution of 5-(methoxymethyl)-1 ,3,4-thiadiazol-2-amine VI (CAS: 15884-86-3, 1 .0 eq., 6.5 g, 45 mmol) in DMF (100 ml_), at 100°C, was added dropwise a solution of 3- bromo-1 , 1 -difluoro-propan-2-one (CAS: 883233-85-0, 1.05 eq., 8.1 g, 47 mmol) in DMF (5 ml_). The reaction mixture was heated at 100°C during 3 h and the completion was checked by LC/MS. A saturated aqueous solution of NaHC03 was added and the organic layer was extracted with ethyl acetate (three times). The combined organic layers were washed with water (five times), dried over MgS04, filtered and evaporated to dryness to give a brown solid (7.6 g). The crude was purified by flash chromatography Biotage Isolera Four (100 g KP-SNAP silica gel column in a gradient of 0% to 5% methanol in dichloromethane over 12 CV) and the pure fractions were evaporated under high vacuum to give 6-(difluoromethyl)-2-(methoxymethyl)imidazo[2, 1 - b][1 ,3,4]thiadiazole VII (3.95 g, 17.8 mmol) as an orange solid. Yield: 40% LC/MS: [M+H]+ = 220.2 1H NMR (400 MHz, DMSO-cfe): δ 8.53 (t, J = 2.2 Hz, 1 H), 7.01 (t, J = 54.6 Hz, 1 H), 4.83 (s, 2H), 3.43 (s, 3H).
40% In water; N,N-dimethyl-formamide at 100℃; for 3h; C.1 C.1. Synthesis of 6-(difluoromethyl)-2-(methoxymethyl)imidazo[2,1-b][1,3,4]thiadiazole VI To a solution of 5-(methoxymethyl)-1,3,4-thiadiazol-2-amine (CAS: 15884-86-3, 1.0 eq., 6.5 g, 45 mmol) in DMF (100 ml_), at 100°C, was added dropwise a solution of 3-bromo- 1,1-difluoro-propan-2-one (CAS: 883233-85-0, 1.05 eq., 8.1 g, 47 mmol) in DMF (5 ml_). The reaction mixture was heated at 100°C during 3 h and the completion was checked by LC/MS. A saturated aqueous solution of NaHCC>3 was added and the organic layer was extracted with ethyl acetate (three times). The combined organic layers were washed with water (five times), dried over MgS04, filtered and evaporated to dryness to give a brown solid (7.6 g). The crude was purified by flash chromatography Biotage Isolera Four (100 g KP-SNAP silica gel column in a gradient of 0% to 5% methanol in dichloromethane over 12 CV) and the pure fractions were combined and evaporated under high vacuum to give 6-(difluoromethyl)-2-(methoxymethyl)imidazo[2,1- b][1,3,4]thiadiazole VI (3.95 g, 17.8 mmol) as an orange solid. Yield: 40% LC/MS: [M+H]+ = 220.2 1H NMR (400 MHz, DMSO-de): d 8.53 (t, J = 2.2 Hz, 1H), 7.01 (t, J = 54.6 Hz, 1H), 4.83 (s, 2H), 3.43 (s, 3H).
 

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